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PharmaCompass offers a list of Dl-Methylephedrine Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Dl-Methylephedrine Hydrochloride manufacturer or Dl-Methylephedrine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dl-Methylephedrine Hydrochloride manufacturer or Dl-Methylephedrine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Dl-Methylephedrine Hydrochloride API Price utilized in the formulation of products. Dl-Methylephedrine Hydrochloride API Price is not always fixed or binding as the Dl-Methylephedrine Hydrochloride Price is obtained through a variety of data sources. The Dl-Methylephedrine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A (1-hydroxy-1-phenylpropan-2-yl)-dimethylazanium;chloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of (1-hydroxy-1-phenylpropan-2-yl)-dimethylazanium;chloride, including repackagers and relabelers. The FDA regulates (1-hydroxy-1-phenylpropan-2-yl)-dimethylazanium;chloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. (1-hydroxy-1-phenylpropan-2-yl)-dimethylazanium;chloride API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A (1-hydroxy-1-phenylpropan-2-yl)-dimethylazanium;chloride supplier is an individual or a company that provides (1-hydroxy-1-phenylpropan-2-yl)-dimethylazanium;chloride active pharmaceutical ingredient (API) or (1-hydroxy-1-phenylpropan-2-yl)-dimethylazanium;chloride finished formulations upon request. The (1-hydroxy-1-phenylpropan-2-yl)-dimethylazanium;chloride suppliers may include (1-hydroxy-1-phenylpropan-2-yl)-dimethylazanium;chloride API manufacturers, exporters, distributors and traders.
click here to find a list of (1-hydroxy-1-phenylpropan-2-yl)-dimethylazanium;chloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a (1-hydroxy-1-phenylpropan-2-yl)-dimethylazanium;chloride Drug Master File in Korea ((1-hydroxy-1-phenylpropan-2-yl)-dimethylazanium;chloride KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of (1-hydroxy-1-phenylpropan-2-yl)-dimethylazanium;chloride. The MFDS reviews the (1-hydroxy-1-phenylpropan-2-yl)-dimethylazanium;chloride KDMF as part of the drug registration process and uses the information provided in the (1-hydroxy-1-phenylpropan-2-yl)-dimethylazanium;chloride KDMF to evaluate the safety and efficacy of the drug.
After submitting a (1-hydroxy-1-phenylpropan-2-yl)-dimethylazanium;chloride KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their (1-hydroxy-1-phenylpropan-2-yl)-dimethylazanium;chloride API can apply through the Korea Drug Master File (KDMF).
click here to find a list of (1-hydroxy-1-phenylpropan-2-yl)-dimethylazanium;chloride suppliers with KDMF on PharmaCompass.
A (1-hydroxy-1-phenylpropan-2-yl)-dimethylazanium;chloride written confirmation ((1-hydroxy-1-phenylpropan-2-yl)-dimethylazanium;chloride WC) is an official document issued by a regulatory agency to a (1-hydroxy-1-phenylpropan-2-yl)-dimethylazanium;chloride manufacturer, verifying that the manufacturing facility of a (1-hydroxy-1-phenylpropan-2-yl)-dimethylazanium;chloride active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting (1-hydroxy-1-phenylpropan-2-yl)-dimethylazanium;chloride APIs or (1-hydroxy-1-phenylpropan-2-yl)-dimethylazanium;chloride finished pharmaceutical products to another nation, regulatory agencies frequently require a (1-hydroxy-1-phenylpropan-2-yl)-dimethylazanium;chloride WC (written confirmation) as part of the regulatory process.
click here to find a list of (1-hydroxy-1-phenylpropan-2-yl)-dimethylazanium;chloride suppliers with Written Confirmation (WC) on PharmaCompass.
(1-hydroxy-1-phenylpropan-2-yl)-dimethylazanium;chloride Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.
GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).
PharmaCompass offers a list of (1-hydroxy-1-phenylpropan-2-yl)-dimethylazanium;chloride GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right (1-hydroxy-1-phenylpropan-2-yl)-dimethylazanium;chloride GMP manufacturer or (1-hydroxy-1-phenylpropan-2-yl)-dimethylazanium;chloride GMP API supplier for your needs.
A (1-hydroxy-1-phenylpropan-2-yl)-dimethylazanium;chloride CoA (Certificate of Analysis) is a formal document that attests to (1-hydroxy-1-phenylpropan-2-yl)-dimethylazanium;chloride's compliance with (1-hydroxy-1-phenylpropan-2-yl)-dimethylazanium;chloride specifications and serves as a tool for batch-level quality control.
(1-hydroxy-1-phenylpropan-2-yl)-dimethylazanium;chloride CoA mostly includes findings from lab analyses of a specific batch. For each (1-hydroxy-1-phenylpropan-2-yl)-dimethylazanium;chloride CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.
(1-hydroxy-1-phenylpropan-2-yl)-dimethylazanium;chloride may be tested according to a variety of international standards, such as European Pharmacopoeia ((1-hydroxy-1-phenylpropan-2-yl)-dimethylazanium;chloride EP), (1-hydroxy-1-phenylpropan-2-yl)-dimethylazanium;chloride JP (Japanese Pharmacopeia) and the US Pharmacopoeia ((1-hydroxy-1-phenylpropan-2-yl)-dimethylazanium;chloride USP).
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